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FDA NDA · NDA009378

CORTEF ACETATE

Sponsor: PHARMACIA AND UPJOHN

APPLICATION
NDA009378
TYPE
NDA
LATEST ACTION
1989-03-22
ROUTE
INJECTION
DOSAGE FORM
INJECTABLE
MARKETING STATUS
Discontinued

Products

CORTEF ACETATEDiscontinued
HYDROCORTISONE ACETATE 50MG/ML · INJECTABLE · INJECTION

Approval history

1989-03-22Labeling · Supplement 20AP
1981-11-10Labeling · Supplement 19AP
1979-09-27Manufacturing (CMC) · Supplement 17 · standardAP
1978-03-07Labeling · Supplement 16AP
1977-05-05Labeling · Supplement 14AP
1977-03-15Manufacturing (CMC) · Supplement 15 · standardAP
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Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.

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